Assay Details
Target Gene Details
Entrez Gene ID: | 55683 |
Gene Name: | KAT8 regulatory NSL complex subunit 3 |
Gene Aliases: |
KIAA1310, NSL3, Rcd1 |
Location: |
Chr.2:96593155-96638379 on Build GRCh38 |
Assay Gene Location: | Within Exon 27 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
KANSL3 | NM_001115016.2 | 21 | 4696 | NP_001108488.1 |
NR_047653.1 | 21 | 4757 | ||
NR_047654.1 | 21 | 4751 | ||
NR_047655.1 | 21 | 4683 | ||
NR_047656.1 | 20 | 4605 | ||
NR_047657.1 | 21 | 4551 | ||
NR_047658.1 | 20 | 4450 | ||
XM_005263984.1 | 22 | 4773 | XP_005264041.1 | |
XM_005263987.1 | 21 | 4689 | XP_005264044.1 | |
XM_017004470.1 | 22 | 4767 | XP_016859959.1 | |
XM_017004473.1 | 22 | 4786 | XP_016859962.1 | |
XM_017004474.1 | 22 | 4681 | XP_016859963.1 | |
AA526958.1 | ||||
AB037731.1 | 21 | 4503 | BAA92548.1 | |
AF311326.1 | 23 | 4503 | AAG33852.1 | |
AK000943.1 | BAA91437.1 | |||
AK023813.1 | 21 | 4718 | BAB14688.1 | |
AK074379.1 | 2 | 2206 | ||
AY050169.1 | 21 | 4724 | AAL13159.1 | |
BC051763.1 | 20 | 4405 | AAH51763.1 | |
BC063792.1 | 21 | 4626 | AAH63792.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
esv2720413 | Chr.2:96472591 - 96793459 on Build GRCh38 | Deletion | CNNM4 LOC105373496 ARID5A NEURL3 FER1L5 LMAN2L KANSL3 |
nsv469775 | Chr.2:96575189 - 96746754 on Build GRCh38 | Loss | FER1L5 LMAN2L KANSL3 |
nsv834306 | Chr.2:96575378 - 96747201 on Build GRCh38 | Loss | FER1L5 LMAN2L KANSL3 |
dgv607e201 | Chr.2:95855884 - 97561622 on Build GRCh38 | Deletion | ANKRD36 LOC105373496 LOC105373495 SEMA4C MIR3127 FAHD2CP LOC653924 CIAO1 ANKRD36C NEURL3 LOC107984110 FER1L5 LMAN2L STARD7 LOC100506076 LOC100506123 FAM178B CNNM4 ARID5A SNRNP200 ITPRIPL1 ANKRD36B ANKRD39 KANSL3 GPAT2 LOC101927053 FAHD2B ANKRD23 ADRA2B DUSP2 NCAPH TMEM127 CNNM3 STARD7-AS1 ASTL |
nsv1135873 | Chr.2:95981454 - 97579645 on Build GRCh38 | Deletion | ANKRD36 LOC105373496 LOC105373495 SEMA4C MIR3127 FAHD2CP LOC653924 CIAO1 ANKRD36C NEURL3 LOC107984110 FER1L5 LMAN2L STARD7 LOC100506076 LOC100506123 FAM178B CNNM4 ARID5A SNRNP200 ITPRIPL1 ANKRD36B ANKRD39 KANSL3 GPAT2 LOC101927053 FAHD2B ANKRD23 ADRA2B DUSP2 NCAPH TMEM127 CNNM3 STARD7-AS1 ASTL |
esv3425717 | Chr.2:95859900 - 97515905 on Build GRCh38 | Duplication | ANKRD36 LOC105373496 LOC105373495 SEMA4C MIR3127 FAHD2CP LOC653924 CIAO1 ANKRD36C NEURL3 LOC107984110 FER1L5 LMAN2L STARD7 LOC100506076 LOC100506123 FAM178B CNNM4 ARID5A SNRNP200 ITPRIPL1 ANKRD36B ANKRD39 KANSL3 GPAT2 LOC101927053 FAHD2B ANKRD23 ADRA2B DUSP2 NCAPH TMEM127 CNNM3 STARD7-AS1 ASTL |
More Information
Set Membership: |
Intragenic Exonic DGV Variation |